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Molecular consequences of dominant Bethlem myopathy collagen VI mutations.
Baker NL, Mörgelin M, Pace RA, Peat RA, Adams NE, Gardner RJ, Rowland LP, Miller G, De Jonghe P, Ceulemans B, Hannibal MC, Edwards M, Thompson EM, Jacobson R, Quinlivan RC, Aftimos S, Kornberg AJ, North KN, Bateman JF, Lamandé SR. Baker NL, et al. Among authors: edwards m. Ann Neurol. 2007 Oct;62(4):390-405. doi: 10.1002/ana.21213. Ann Neurol. 2007. PMID: 17886299
Premature arthritis is a distinct type II collagen phenotype.
Kannu P, Bateman JF, Randle S, Cowie S, du Sart D, McGrath S, Edwards M, Savarirayan R. Kannu P, et al. Among authors: edwards m. Arthritis Rheum. 2010 May;62(5):1421-30. doi: 10.1002/art.27354. Arthritis Rheum. 2010. PMID: 20131279 Free article.
Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA.
van Kogelenberg M, Clark AR, Jenkins Z, Morgan T, Anandan A, Sawyer GM, Edwards M, Dudding T, Homfray T, Castle B, Tolmie J, Stewart F, Kivuva E, Pilz DT, Gabbett M, Sutherland-Smith AJ, Robertson SP. van Kogelenberg M, et al. Among authors: edwards m. J Mol Med (Berl). 2015 Jul;93(7):773-82. doi: 10.1007/s00109-015-1261-7. Epub 2015 Feb 18. J Mol Med (Berl). 2015. PMID: 25686753
Perspectives on the diagnosis and management of functional cognitive disorder: An international Delphi study.
Cabreira V, Alty J, Antic S, Araújo R, Aybek S, Ball HA, Baslet G, Bhome R, Coebergh J, Dubois B, Edwards M, Filipović SR, Frederiksen KS, Harbo T, Hayhow B, Howard R, Huntley J, Isaacs J, LaFrance WC Jr, Larner AJ, Di Lorenzo F, Main J, Mallam E, Marra C, Massano J, McGrath ER, McWhirter L, Moreira IP, Nobili F, Pennington C, Tábuas-Pereira M, Perez DL, Popkirov S, Rayment D, Rossor M, Russo M, Santana I, Schott J, Scott EP, Taipa R, Tinazzi M, Tomic S, Toniolo S, Tørring CW, Wilkinson T, Frostholm L, Stone J, Carson A. Cabreira V, et al. Among authors: edwards m. Eur J Neurol. 2024 May 3:e16318. doi: 10.1111/ene.16318. Online ahead of print. Eur J Neurol. 2024. PMID: 38700361
5,043 results